Léa Baudoin

ORCID: 0000-0002-5487-9191
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About
Contact & Profiles
Research Areas
  • Carbohydrate Chemistry and Synthesis
  • Galectins and Cancer Biology
  • Glycosylation and Glycoproteins Research
  • Systemic Sclerosis and Related Diseases
  • Dermatologic Treatments and Research
  • Oil Palm Production and Sustainability
  • Agriculture and Rural Development Research
  • Hair Growth and Disorders
  • Autoimmune Bullous Skin Diseases
  • African Botany and Ecology Studies

Institut Cochin
2016-2020

Université Paris Cité
2019-2020

Inserm
2016-2020

Centre National de la Recherche Scientifique
2019-2020

Sorbonne Paris Cité
2019

Abstract Glycosylation with O-linked β-N-acetylglucosamine (O-GlcNAcylation) is a reversible posttranslational modification that regulates the activity of intracellular proteins according to glucose availability and its metabolism through hexosamine biosynthesis pathway. This has been involved in regulation various immune cell types, including macrophages. However, little known concerning mechanisms regulate protein O-GlcNAcylation level these cells. In present work, we demonstrate LPS...

10.4049/jimmunol.2000345 article EN The Journal of Immunology 2020-09-25

Abstract O-GlcNAc glycosylation is a reversible post-translational modification that regulates the activity of intracellular proteins according to glucose availability and its metabolism through hexosamine biosynthesis pathway (HBP). This has been involved in regulation various immune cell types, including macrophages. However, little known concerning mechanisms regulate protein O-GlcNAcylation level these cells. In present work, we demonstrate LPS treatment induces marked increase RAW264.7...

10.1101/2020.03.22.002303 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-03-23

<h3>Background</h3> Systemic sclerosis (SSc) primarily affects postmenopausal women. This sex bias could partly be explained by the action of estrogens on immune system and/or fibrogenesis. Since little is known about their direct role in <h3>Objectives</h3> Our aim was to evaluate effects i) pathological activation dermal fibroblasts induced transforming growth factor-b (TGF-β) and ii) development experimental fibrosis. <h3>Methods</h3> Effects estrogen inhibition gene inactivation...

10.1136/annrheumdis-2016-eular.2835 article EN Annals of the Rheumatic Diseases 2016-06-01
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